Cas 910783-88-9,4,4,5,5-tetramethyl-2-(4-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-1-en-2-yl)-1,3,2-dioxaborolane

910783-88-9

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Basic information

Product Name: 4,4,5,5-tetramethyl-2-(4-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-1-en-2-yl)-1,3,2-dioxaborolane
Synonyms: 4,4,5,5-tetramethyl-2-(4-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-1-en-2-yl)-1,3,2-dioxaborolane
CAS NO:910783-88-9
Molecular Formula:
Molecular Weight: 384.132
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4,4,5,5-tetramethyl-2-(4-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-1-en-2-yl)-1,3,2-dioxaborolane(CAS DataBase Reference)
NIST Chemistry Reference: 4,4,5,5-tetramethyl-2-(4-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-1-en-2-yl)-1,3,2-dioxaborolane(910783-88-9)
EPA Substance Registry System: 4,4,5,5-tetramethyl-2-(4-phenyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)but-1-en-2-yl)-1,3,2-dioxaborolane(910783-88-9)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 910783-88-9(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 910783-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,1,0,7,8 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 910783-88:
(8*9)+(7*1)+(6*0)+(5*7)+(4*8)+(3*3)+(2*8)+(1*8)=179
179 % 10 = 9
So 910783-88-9 is a valid CAS Registry Number.

910783-88-9Upstream product

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910783-88-9Relevant academic research and scientific papers

Modular asymmetric synthesis of 1,2-diols by single-pot allene diboration/hydroboration/cross-coupling

Pelz, Nicholas F.,Morken, James P.

, p. 4557 - 4559 (2006)

Chiral allyl vinyl boronates are generated by catalytic enantioselective diboration of prochiral allenes. They may then be reacted, in situ, with a hydroborating reagent to form a novel triboron intermediate. The least hindered and most reactive C-B bond

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